ライフサイエンスコーパス: goodness-of-fit test

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1 e (A) (purine to purine) (p<0.001, Pearson's goodness-of-fit test).

2 bration (P = .33 vs P = .02, Hosmer-Lemeshow goodness-of-fit test).

3 ating characteristic curve) and calibration (goodness-of-fit testing).

4 E are commonly performed using a simple chi2 goodness-of-fit test.

5 tests, the chi 2 and the Kolmogorov-Smirnov goodness of fit tests.

6 g control, compared with the C statistic and goodness-of-fit tests.

7 assessed through prediction diagnostics and goodness-of-fit tests.

8 libration was assessed using Hosmer-Lemeshow goodness-of-fit tests.

9 tatus Epilepticus Severity Score (chi-square goodness-of-fit test = 1.39; p = 0.845).

10 From the goodness-of-fit test, a critical percentage for each adm

11 These model fits can pass a host of standard goodness-of-fit tests and other model-selection diagnost

12 Goodness-of-fit tests and receiver operating characteris

13 tes of heritability; and (iv) we developed a goodness of fit test based on the correlation of viral l

14 (discrimination) and by the Hosmer-Lemeshow goodness-of-fit test (calibration).

15 well as good calibration (as measured by the goodness-of-fit test comparing observed to expected coun

16 We also propose a goodness-of-fit test for discriminating rejections due t

17 d by this problem we propose a nonparametric goodness-of-fit test for two empirical distributions of

18 el C index) and calibration (Hosmer-Lemeshow goodness-of-fit test) for prediction of in-hospital and

19 However, goodness-of-fit tests found that even bounded power-law

20 y of observed against predicted outcomes and goodness-of-fit test indicated good calibration of the s

21 The three-level goodness-of-fit test indicated satisfactory performance

22 Goodness-of-fit testing indicated excellent model calibr

23 Segregation analysis and goodness-of-fit testing of genetic models suggest that r

24 ve of 0.80) and calibration (Hosmer-Lemeshow goodness-of-fit test, P = 0.102) when applied to the ADR

25 monstrated good calibration (Hosmer-Lemeshow goodness-of-fit test, P = 0.71) and discrimination (c-st

26 e show, however, that despite passing common goodness-of-fit tests, PP-GLMs estimated from data are o

27 Surprisingly, goodness-of-fit tests reveal that this class of phenotyp

28 A goodness-of-fit test revealed that DR-DQ haplotype shari

29 ing 1- and 2-tissue-compartment models, with goodness-of-fit tests showing a preference for the 2-tis

30 e representation of data, which are based on goodness-of-fit test statistics and standard errors of p

31 Goodness-of-fit tests strongly supported the fit of the

32 The goodness-of-fit test suggests that the phylogenetic mode

33 atio test of selection in conjunction with a goodness-of-fit test supports the selection hypothesis o

34 We also propose a goodness-of-fit test to aid investigators in determining

35 or the observed number of conversions, and a goodness-of-fit test to compare the observed number of c

36 evaluate discrimination and Hosmer-Lemeshow goodness-of-fit tests to evaluate calibration.

37 Using a chi-squared goodness-of-fit test, we identified 10 amino acid sites

38 (T classes vs. T + 1 classes) and chi-square goodness-of-fit tests were evaluated using parametric bo

39 Goodness-of-fit tests were more sensitive than the recei

40 g and validation samples as indicated by the goodness-of-fit test, which evaluated standardized nosoc

41 f the validity of a scoring system--and chi2 goodness-of-fit testing with data from 197 patients.

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